Evidence map›Paper›PMID 42552364›Full record

ArticleBritish journal of cancer2026

A Phase 1/2 study of ontorpacept (TTI-621) in combination with doxorubicin in patients with unresectable or metastatic high-grade leiomyosarcoma.

Sujana Movva, Victoria Allgood, Rashmi Chugh, Lara E Davis, Howard H Bailey, Mohammed Milhem, Varun Monga, Steven Attia, Ankit Mangla, Ingmar Bruns and 8 more

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Article in British journal of cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors.

Sujana MovvaMemorial Sloan Kettering Cancer Center, New York, NY, USA. movvas@mskcc.org.ORCID http://orcid.org/0000-0002-6569-6606
Victoria AllgoodFormer Pfizer Employee, San Antonio, TX, USA.
Rashmi ChughUniversity of Michigan, Rogel Comprehensive Cancer Center, Ann Arbor, MI, USA.
Lara E DavisKnight Cancer Institute, Oregon Health and Science University, Portland, OR, USA.
Howard H BaileyUniversity of Wisconsin Carbone Cancer Center, Madison, WI, USA.
Mohammed MilhemUniversity of Iowa Hospitals and Clinics, Iowa City, IA, USA.
Varun MongaUniversity of California, San Francisco, CA, USA.
Steven AttiaDepartment of Hematology and Oncology, Mayo Clinic, Jacksonville, FL, USA.
Ankit ManglaUniversity Hospitals Seidman Cancer Center-Case Western Reserve University Case Comprehensive Cancer Center, Cleveland, OH, USA.
Ingmar BrunsFormer Pfizer Employee, San Antonio, TX, USA.
Luke KuttschreuterFormer Pfizer Employee, San Antonio, TX, USA.
Dalila Bouyoucef-CherchalliPfizer Inc, Great Britain, Surrey, UK.
Caimiao WeiPfizer Inc, Groton, CT, USA.
Gloria H Y LinPfizer Canada ULC, Quebec, CT, USA.
Hong ZhangPfizer Inc, New York, NY, USA.
Ilan PomeranceMemorial Sloan Kettering Cancer Center, New York, NY, USA.
Mihaela DrutaMoffitt Cancer Center, Tampa, FL, USA.
Sant ChawlaSarcoma Oncology Center, Santa Monica, CA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOntorpacept, a recombinant signal regulatory protein alpha (SIRPα)-blocking fusion protein, has antitumour activity by disrupting CD47-SIRPα signalling. This Phase 1/2 study examined ontorpacept with doxorubicin in patients with leiomyosarcoma.

methodsEligible patients were ≥18 years with metastatic or locally advanced high-grade soft-tissue sarcomas (high-grade leiomyosarcoma in Phase 2). In Phase 1, patients received escalating doses of ontorpacept plus doxorubicin. Phase 2 dose expansion evaluated ontorpacept doses 0.2, 1.0, and 2.0 mg/kg plus doxorubicin. The primary endpoints were safety (Phase 1); and objective response rate (ORR) (Phase 1/2).

resultsSeventy-six patients were enrolled (Phase 1, n = 9; Phase 2, n = 67). No dose-limiting toxicities occurred in Phase 1. The most common treatment-related adverse events were neutrophil count decreased/neutropenia (grade ≥3 in 66% of patients). In Phase 1, one patient receiving ontorpacept 2.0 mg/kg had a confirmed partial response. In Phase 2, six patients receiving ontorpacept 0.2 mg/kg (ORR, 18.8%; 95% CI, 7.2-36.4) and one patient receiving 2.0 mg/kg (ORR, 4.5%; 95% CI, 0.1-22.8) had confirmed partial responses.

conclusionsThis first study of CD47 inhibition with chemotherapy in leiomyosarcomas shows manageable safety, supporting further investigation of ontorpacept dosing and schedule, in combination with doxorubicin and as monotherapy.

Identifiers

PMID42552364

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.